Lisinopril - 24658-241-10 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 24658-241
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 5    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 24658-241
Labeler Name: Blu Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076063
Marketing Category: ANDA
Start Marketing Date: 20090202

Package Information of Lisinopril

Package NDC: 24658-241-10
Package Description: 1000 TABLET in 1 BOTTLE (24658-241-10)

NDC Information of Lisinopril

NDC Code 24658-241-10
Proprietary Name Lisinopril
Package Description 1000 TABLET in 1 BOTTLE (24658-241-10)
Product NDC 24658-241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090202
Marketing Category Name ANDA
Labeler Name Blu Pharmaceuticals, LLC
Substance Name LISINOPRIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information